US2024343660A1PendingUtilityA1
Improved systems and processes for high-selectivity conversion of mono-aromatics from olefins
Est. expiryAug 12, 2041(~15.1 yrs left)· nominal 20-yr term from priority
C07C 2529/04C07C 4/06C10G 50/00B01J 29/90C10K 1/003C10K 1/004C10K 1/02C10K 1/10C10K 1/12C10K 1/20B01J 29/405C10J 2300/1659C10J 2300/1656C10J 2300/0916C10J 2300/093C10J 2300/0946C07C 2529/40C07C 2/42
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Claims
Abstract
The disclosure related to processes for the high-selectivity conversion of olefins to monocyclic aromatic compounds, such as BTX, via the introduction of a weakly coordinating compound to a dehydroaromatization catalyst. Moreover, certain embodiments relate to processes for recycling polyaromatic compounds back to a reactor to improve the yield of said monocyclic aromatic compounds. Moreover, certain embodiments relate to processes for regenerating the dehydroaromatization catalyst.
Claims
exact text as granted — not AI-modified1 . A process for high-selectivity conversion of a first composition comprising olefins to a second composition comprising at least one monocyclic aromatic compound, comprising the steps of:
a) introducing the first composition to at least one catalyst capable of converting olefins to at least one monocyclic aromatic compound; b) operating said process using a reactor at high severity to result in the production of at least one monocyclic aromatic compound; and at least one of: c) introducing at least one weakly coordinating compound to the catalyst; and c2) forming at least one polyaromatic compound in said process, wherein said at least one polyaromatic compound is recycled to a gasifier or pyrolysis reactor or catalytic reactor.
2 . The process according to claim 1 , further comprising the step of subjecting the first composition with a nitrogen and/or sulfur atom and/or halogen-containing compound removal process.
3 . (canceled)
4 . The process according to claim 1 , wherein said at least one catalyst is porous aluminosilicate or zeolitic material with a portion of its pores in the micro-, meso- and/or macro-range.
5 . The process according to claim 1 , wherein said at least one catalyst is subject to a regeneration process, wherein said regeneration process comprises the introduction of inert gas and/or an oxidant and/or a reductive fluid.
6 . The process according to claim 4 , wherein said high severity is in an outlet or inlet of said reactor, or intra-reactor, and further wherein said high severity is greater than 425° C..
7 . The process according to claim 6 , wherein said weakly-coordinating compound reduces the H—O bond frequency of the zeolite or aluminosilicate framework by about 1 to 300 cm −1 as measured by FT-IR.
8 . The process according to claim 1 , wherein said olefins have a carbon chain length of C2 to C4.
9 . (canceled)
10 . (canceled)
11 . The process according to claim 1 , further comprising the step of removing at least one by-product before introducing the first composition to at least one zeolitic catalyst.
12 . The process according to claim 11 , wherein said at least one by-product is removed by adsorption, aqueous redox reaction, solvent or solid absorption, electrostatic precipitation, centrifugal separation, or filtration.
13 . (canceled)
14 . (canceled)
15 . The process according to claim 1 , wherein said high-selectivity conversion of a first composition comprising olefins to a second composition comprising the monocyclic aromatic compounds is greater than 25.
16 . (canceled)
17 . The process of claim 1 , further comprising: subjecting a feed gas to a compound removal process to yield the first composition, the compound removal process comprising:
inputting the feed gas and a compound removal solution into a compound removal reactor; and outputting from the reactor an output including the first composition.
18 . The process of claim 17 , the compound removal solution including:
circulating ammonium polysulfide (APS); diammonium polysulfide; ammonium hydroxide; or a mixture thereof.
19 . (canceled)
20 . (canceled)
21 . The process of claim 17 , the compound removal solution including a mixture of a first compound removal solution component and a second compound removal solution component in aqueous solution at a weight ratio of 1:2 at approximately 20-40° C., wherein the second compound removal solution component is an alkaline component.
22 . A process for supplying a first composition to a downstream catalytic process, comprising:
inputting the feed gas and a compound removal solution into a compound removal contactor; and operating the reactor to remove at least one by-product from the feed gas; and, outputting from the reactor an output composition to the downstream catalytic process, the output composition including at least one olefin.
23 . The process of claim 22 , the compound removal solution including:
circulating ammonium polysulfide (APS); diammonium polysulfide; ammonium hydroxide; or a combination thereof.
24 . (canceled)
25 . (canceled)
26 . The process of claim 22 , the compound removal solution including a mixture of a first compound removal solution component and a second compound removal solution component in aqueous solution at a weight ratio of 1:2 at approximately 20-40° C.
27 . The process of claim 22 , further comprising:
outputting from the compound removal contactor an additional output including a by-product removal output; stripping at least one component of the by-product removal output in a vessel separate from the reactor.
28 . The process of claim 27 , the by-product removal output including ammonium polysulfide (APS).
29 . The process of claim 28 , the at least one component of the by-product removal output including gaseous ammonia and hydrogen sulfide.
30 . (canceled)
31 . (canceled)
32 . The process of claim 27 , the at least one component including ammonium polysulfide (APS), the process further comprising circulating the APS to the compound removal contactor.Join the waitlist — get patent alerts
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